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Phenotypes Associated with This Genotype
Genotype
MGI:5431943
Allelic
Composition
Ptentm1Rdp/Ptentm1Rdp
Terttm1Rdp/Terttm1Rdp
Trp53tm1Brn/Trp53tm1Brn
Tg(Pbsn-cre)4Prb/0
Genetic
Background
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptentm1Rdp mutation (0 available); any Pten mutation (86 available)
Terttm1Rdp mutation (0 available); any Tert mutation (55 available)
Tg(Pbsn-cre)4Prb mutation (2 available)
Trp53tm1Brn mutation (20 available); any Trp53 mutation (237 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• at generations 3 and 4 (G3/4), all mice develop smaller, poorly progressive tumors compared to G0 mice
• high-grade prostate intraepithelial neoplasia (HPIN) in all mice by 9 weeks of age
• most tumors fail to progress beyond HPIN by 24 weeks of age unlike in G0 mice
• smaller, poorly progressive tumors compared to tumors in G0 mice
• markedly increased apoptosis and decreased proliferation in tumor cells compared tumor cells from G0 mice

endocrine/exocrine glands
• at generations 3 and 4 (G3/4), all mice develop smaller, poorly progressive tumors compared to G0 mice
• high-grade prostate intraepithelial neoplasia (HPIN) in all mice by 9 weeks of age
• most tumors fail to progress beyond HPIN by 24 weeks of age unlike in G0 mice

cellular
• reduced at G3/4

reproductive system
• at generations 3 and 4 (G3/4), all mice develop smaller, poorly progressive tumors compared to G0 mice
• high-grade prostate intraepithelial neoplasia (HPIN) in all mice by 9 weeks of age
• most tumors fail to progress beyond HPIN by 24 weeks of age unlike in G0 mice


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/20/2026
MGI 6.24
The Jackson Laboratory